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ICF syndrome (medical condition): A very rare, recessively inherited syndrome...more »
See also:
ICF syndrome:
»Introduction: ICF syndrome
»Symptoms of ICF syndrome
»Treatments for ICF syndrome
ICF syndrome: Variable immunodeficiency with centromeric instability of chromosomes 1, 9, 16 and, less frequently, chromosome 2. Manifestations vary and most common symptoms include facial dysmorphism, mental retardation and prolonged respiratory, cutaneous, and gastrointestinal infections.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for ICF syndrome:
ICF syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that ICF syndrome, or a subtype of ICF syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list ICF syndrome as a "rare disease".
Source - Orphanet
ICF syndrome (medical condition): See ICF syndrome (disease information).
»Introduction: ICF syndrome
»Symptoms of ICF syndrome
»Treatments for ICF syndrome
ICF syndrome: ICF syndrome is listed as a type of (or associated with) the following medical conditions in our database:
Source: Diseases Database
Source - NIH
Source: Diseases Database
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